Blood group antigen profile predicted by molecular biology - Use of real-time polymerase chain reaction to genotype important KEL, JK, RHD, and RHCE alleles

Immunohematology

Volumn 18, Issue 3, 2002, Pages 59-64

  Araújo, Fernando ^a   Pereira, C ^a   Monteiro, F ^a   Henriques, I ^a   Meireles, E ^a   Lacerda, P ^a   Aleixo, A ^a   Rodrigues, M J ^a   Celeste, R ^a   Cunha Ribeiro, L M ^a  

^a NONE   (Portugal)

Author keywords

JK; KEL; LightCycler; Real time PCR; RHCE; RHD

Indexed keywords

ALLOANTIBODY; BLOOD GROUP ANTIGEN; DNA;

ALLELE; ARTICLE; BLOOD DONOR; BLOOD GROUP KELL SYSTEM; BLOOD GROUP KIDD SYSTEM; BLOOD GROUP RH; BLOOD GROUP SYSTEM; BLOOD TRANSFUSION; BLOOD TRANSFUSION REACTION; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; NEWBORN HEMOLYTIC DISEASE; NUCLEOTIDE SEQUENCE; PHENOTYPE; POLYMERASE CHAIN REACTION; PREGNANCY; PRIORITY JOURNAL; SEROLOGY;

EID: 0036375099     PISSN: 0894203X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (23)

1. Cartron JP, Colin Y. Structural and functional diversity of blood group antigens. Transfus Clin Biol 2001;8:163-99.
2. Reid ME, Rios M, Powell VI, Charles-Pierre D, Malavade V. DNA from blood samples can be used to genotype patients who have recently received a transfusion. Transfusion 2000;40:48-53.
3. Rozman P, Dovc T, Gassner C. Differentiation of autologous ABO, RHD, RHCE, KEL, JK, and FY blood group genotypes by analysis of peripheral blood samples of patients who have recently received multiple transfusions. Transfusion 2000;40:936-42.
4. Lee S, Wu X, Reid M, Zelinski T, Redman C. Molecular basis of the Kell (K1) phenotype. Blood 1995;85:912-6.
5. Hessner MJ, McFarland JG, Endean DJ. Genotyping of KEL1 and KEL2 of the human Kell blood group system by the polymerase chain reaction with sequence-specific primers. Transfusion 1996;36:495-9.
6. Lee S, Wu S, Son S, et al. Point mutations characterize KEL10, the KEL3, KEL4, and KEL21 alleles, and the KEL7 and KEL11 alleles. Transfusion 1996;36:490-4.
7. Lee S. Molecular basis of Kell blood group phenotypes. Vox Sang 1997;73:1-11.
8. Heaton DC, McLoughlin K. Jk(a-b-) red blood cells resist urea lysis. Transfusion 1982;22:70-1.
9. Frohlich O, Macey RI, Edwards-Moulds J, Gargus JJ, Gunn RB. Urea transport deficiency in Jk(a-b-) erythrocytes. Am J Physiol 1991;260:C778-83.
10. Olivés B, Merriman M, Bailly P, et al. The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility. Hum Mol Genet 1997;6:1017-20.
11. Irshaid NM, Thuresson B, Olsson ML. Genomic typing of the Kidd blood group locus by a single-tube allele specific primer PCR technique. Br J Haematol 1998;102:1010-4.
12. Sidoux-Walter F, Lucien N, Nissinen R, et al. Molecular heterogeneity of the Jk-null phenotype: expression analysis of the Jk S291P mutation found in Finns. Blood 2000;96:1566-73.
13. Irshaid NM, Henry SM, Olsson ML. Genomic characterization of the Kidd blood group gene: different molecular basis of the Jk(a-b-) phenotypes in Polynesians and Finns. Transfusion 2000;40:69-74.
14. Lucient N, Sidoux-Walter F, Olivés B, et al. Characterization of the gene encoding the human Kidd blood group/urea transporter protein. J Biol Chem 1998;273:12973-80.
15. Cartron JP, Bailly P, Le Van Kim C, et al. Insights into the structure and function of membrane polypeptides carrying blood group antigens. Vox Sang 1998;74(Suppl 2):29-64.
16. Gassner C, Schmarda A, Kilga-Nogler S, et al. RHD/CE typing by polymerase chain reaction using sequence-specific primers. Transfusion 1997;37:1020-6.
17. Le Van Kim C, Mouro I, Brossard Y, Chavinié J, Cartron JP. PCR-based determination of Rhc and RhE status of fetuses at risk of Rhc and RhE haemolytic disease. Br J Haematol 1994;88:193-5.
18. Singleton BK, Green CA, Avent ND, et al. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype. Blood 2000;95:12-8.
19. Simsek S, Faas BHW Bleeker PMM, et al. Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA. Blood 1995;85:2975-80.
20. Vaughan J, Manning M, Warwick R, Letsky EA, Murray NA, Roberts IAG. Inhibition of erythroid progenitor cells by anti-Kell antibodies in fetal alloimmune anemia. N Engl J Med 1996;338:798-803.
21. Wylenzek M, Geisen C, Stapenhorst L, Wielckens K, Klinger KR. A novel point mutation in the 3′ region of the prothrombin gene at position 20221 in a Lebanese/Syrian family. Thromb Haemost 2001;85:943-4.
22. Kroll H, Carl B, Santoso S, Bux J, Bein G. Workshop report on the genotyping of blood cell alloantigens. Transfus Med 2001;11:201-9.
23. Araújo F, Pereira C, Aleixo A, et al. Rapid genotyping of the major alleles at the Duffy (FY) blood group locus using real-time fluorescence polymerase chain reaction. Immunohematology 2001;17:42-4.